[Federal Register Volume 72, Number 184 (Monday, September 24, 2007)]
[Rules and Regulations]
[Page 54208]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E7-18799]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 610

[Docket No. 2007N-0264]


Revisions to the Requirements Applicable to Blood, Blood 
Components and Source Plasma; Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Direct final rule; correction.

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SUMMARY: The Food and Drug Administration is correcting a direct final 
rule that appeared in the Federal Register of August 16, 2007 (72 FR 
45883). That document amended the biologics regulations by removing, 
revising, or updating specific regulations applicable to blood, blood 
components and Source Plasma to be more consistent with current 
practices in the blood industry and to remove unnecessary or outdated 
requirements. A proposal was published as a companion document to the 
direct final rule in the same issue of the Federal Register (August 16, 
2007, 72 FR 45993). Both documents published with a typographical error 
in the codified section. This document corrects the error in the direct 
final rule. Elsewhere in this issue of the Federal Register we are 
correcting the error in the proposed rule.

DATES: This correction is effective February 19, 2008.

FOR FURTHER INFORMATION CONTACT:
    For information regarding this correction: Joyce Strong, Office of 
Policy (HF-27), Food and Drug Administration, 5600 Fishers Lane, 
Rockville, MD 20857, 301-827-7010.
    For information regarding the direct final rule: Stephen M. Ripley, 
Center for Biologics Evaluation and Research (HFM-17), Food and Drug 
Administration, 1401 Rockville Pike, Rockville, MD 20852-1448, 301-827-
6210.

SUPPLEMENTARY INFORMATION: In FR Doc. E7-15943, appearing on page 
45883, in the Federal Register of Thursday, August 16, 2007, the 
following correction is made:


Sec.  610.53  [Corrected]

0
1. On page 45887, in the amendment to Sec.  610.53 Dating periods for 
licensed biological products, in the table in paragraph (c), ``65[deg] 
C'' is corrected to read ``-65[deg] C'' everywhere it appears.

    Dated: September 17, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7-18799 Filed 9-21-07; 8:45 am]
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